The Recall Desk

State

South Carolina product recalls

73,827 recalls have nationwide distribution and so reach South Carolina. 7,153 additional recalls listed South Carolina specifically in their distribution scope.

What the numbers show

Total
7,153
Critical
1,275
Severe
2,170
Most recent
2026-11-04

Of the 7,153 recalls naming South Carolina we have scored against our rubric, 1,275 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,170 (30%) are Severe.

These figures cover only the 7,153 recalls whose distribution notice names South Carolina specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

54051–54075 of 80980

  • HighNHTSA·16V298000·2016-05-13

    Supreme Classic American Trolley Recall for Seat Belt Anchor Weld Defect

    Supreme is recalling 2010-2016 Classic American Trolley vehicles because missing welds on seat brackets may allow seat belt anchors to separate, increasing injury risk in a crash.

    Product
    SUPREME — SUPREME CLASSIC AMERICAN TROLLEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V295000·2016-05-12

    Champion Challenger Shuttle Buses Recalled for Seat Separation Risk

    Champion is recalling 2016 Challenger shuttle buses because seats may separate from the base frame due to bolt failure, increasing injury risk in a crash.

    Product
    CHAMPION — CHAMPION CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V293000·2016-05-12

    E-One Recalls 2015-2016 Emergency Vehicles Due to Pump Strainer Defect

    E-One is recalling 140 model year 2015-2016 Cyclone II, Quest II, and Typhoon emergency vehicles because pump intake strainers may be improperly soldered.

    Product
    E-ONE — E-ONE CYCLONE II, QUEST II, TYPHOON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V294000·2016-05-12

    Kovatch Mobile Equipment Recalls Firefighting Vehicles Due to Pump Strainer Defect

    Kovatch Mobile Equipment is recalling certain 2016-2017 emergency vehicles because pump intake strainers may be improperly soldered, potentially causing pump damage and reduced firefighting effectiveness.

    Product
    NAVISTAR — NAVISTAR, KME 4400, 7400, PREDATOR SS, PREDATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V296000·2016-05-12

    Supreme Recalls 2011-2014 Vans Due to Fire Risk in Marker Lights

    Supreme Corporation is recalling 2011-2014 Signature Van, Iner-City, and Kold King vehicles because roof marker lights may short circuit and cause the corner caps to catch fire.

    Product
    SUPREME — SUPREME KOLD KING, INER-CITY, SIGNATURE VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1318-2016·2016-05-11

    Back To Nature Classic Creme Cookies Recalled for Undeclared Milk

    Back To Nature Foods is recalling Classic Creme Cookies because they contain undeclared milk. The recall covers 154,044 cartons shipped to 16 states.

    Product
    Classic Creme Cookies, Net wt. 12 oz cartons, 6 cartons per case. Manufactured for Back To Nature Foods Co., LLC
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1535-2016·2016-05-11

    B Braun Recalls Dialog+ Hemodialysis Conductivity Sensors Due to Leakage Risk

    B Braun Medical Inc is recalling 68 Dialog+ Hemodialysis Conductivity Sensors due to a potential leakage hazard. The units were distributed nationwide to various states and territories.

    Product
    Dialog+ Hemodialysis machines: Conductivity Sensor (BIC) Item # 3456102A The Dialog+ can be used for implementing and monitoring hemodialysis treatments for patients with acute or chronic kidney failure. The system can be used in hospital, health center and outpatient dialysis…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1320-2016·2016-05-11

    Kroger Raw Macadamia Nuts Recalled Due to Salmonella Contamination

    The Kroger Company is recalling raw macadamia nuts after positive Salmonella test results. Consumers should check their pantries for the specific UPC and sell-by date.

    Product
    Kroger Raw #4 Macadamia Nuts. UPC 2 04192 51053 2 Dist. by the Kroger Company Cincinnati, Ohio 45202
    Category
    Food
    Distribution
    18 states
  • SevereNHTSA·16V291000·2016-05-11

    Keystone Recalls 2016-2017 Passport Trailers Due to Axle Defect

    Keystone RV Company is recalling specific 2016-2017 Passport trailers because they were built with axles that have lower capacity than required, increasing the risk of axle failure and a crash.

    Product
    KEYSTONE — KEYSTONE PASSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1531-2016·2016-05-11

    B Braun Recalls Dialog+ Hemodialysis Machines Due to Sensor Leakage Risk

    B Braun Medical Inc is recalling 370 Dialog+ Hemodialysis machines because conductivity sensors may leak. The recall covers units distributed nationwide and in Puerto Rico.

    Product
    Dialog+ Hemodialysis machines: Dialog A + HE/BIC Product Code 710200L Serial # >200318 and < 2039222 The Dialog+ can be used for implementing and monitoring hemodialysis treatments for patients with acute or chronic kidney failure. The system can be used in hospital, health…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1536-2016·2016-05-11

    B Braun Recalls Dialog+ Hemodialysis Conductivity Sensors Due to Leakage Risk

    B Braun Medical Inc is recalling 147 Dialog+ Hemodialysis Conductivity Sensors due to potential leakage. The sensors are used in dialysis machines for kidney failure patients.

    Product
    Dialog+ Hemodialysis machines: Conductivity Sensor (BIC) Item 3456103A The Dialog+ can be used for implementing and monitoring hemodialysis treatments for patients with acute or chronic kidney failure. The system can be used in hospital, health center and outpatient dialysis…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1534-2016·2016-05-11

    B Braun Recalls Dialog+ Hemodialysis Machines Due to Sensor Leakage Risk

    B Braun Medical Inc is recalling 90 Dialog+ Hemodialysis machines because conductivity sensors may leak. The recall covers units distributed nationwide.

    Product
    Dialog+ Hemodialysis machines: Dialog + 120 V DF+Adimea+WAN-BSL-BIC Product Code # 710200U Serial # 202136 and < 203837 The Dialog+ can be used for implementing and monitoring hemodialysis treatments for patients with acute or chronic kidney failure. The system can be used in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1317-2016·2016-05-11

    NORVEN Herring in Oil Recalled for Listeria Contamination

    OLMA-XXI Inc. is recalling NORVEN herring in oil due to Listeria monocytogenes contamination found by FDA sampling.

    Product
    NORVEN herring in oil, Net Wt. 17.6 oz. (500g), UPC barcode 856687004196, and Net Wt. 10.6 oz. (300g), UPC barcode 856687004189 -- Product of Ukraine -- Distributed by: OLMA-XXI Inc. 204 28th Street, Brooklyn, NY 11232
    Category
    Food
    Distribution
    13 states
  • SevereNHTSA·16V284000·2016-05-11

    2016 Jeep Cherokee Recall for Right Halfshaft Fracture Risk

    Chrysler is recalling 2016 Jeep Cherokee vehicles because the right halfshaft may fracture without warning, increasing crash risk.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1532-2016·2016-05-11

    B Braun Dialog+ Hemodialysis Machines Recalled for Potential Sensor Leakage

    B Braun Medical Inc. is recalling 40 Dialog+ Hemodialysis machines due to a potential leakage issue with conductivity sensors.

    Product
    Dialog+ Hemodialysis machines: Dialog A + 1 Blood Pump 120V Product Code 710200K Serial # >202169 and < 203249 The Dialog+ can be used for implementing and monitoring hemodialysis treatments for patients with acute or chronic kidney failure. The system can be used in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1533-2016·2016-05-11

    B Braun Recalls Dialog+ Hemodialysis Machines Due to Sensor Leakage

    B Braun Medical Inc is recalling 318 Dialog+ Hemodialysis machines because conductivity sensors may leak. The recall covers units distributed nationwide.

    Product
    Dialog+ Hemodialysis machines: Dialog + 120 V DF+Adimea+WAN-BSL Product Code # 710200S Serial # >200805 and <204001 The Dialog+ can be used for implementing and monitoring hemodialysis treatments for patients with acute or chronic kidney failure. The system can be used in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V292000·2016-05-11

    Subaru Recalls 2016-2017 Legacy and Outback for Steering Column Defect

    Subaru is recalling 48,819 Legacy and Outback vehicles because an improperly machined steering column may cause loss of steering control, increasing crash risk.

    Product
    SUBARU — SUBARU OUTBACK, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·040-2016·2016-05-11

    Ajinomoto Windsor Recalls Meat and Poultry Products Due to Listeria Risk

    Ajinomoto Windsor is recalling approximately 47 million pounds of not-ready-to-eat meat and poultry products due to possible Listeria monocytogenes contamination.

    Product
    Ajinomoto Windsor Inc. — Ajinomoto Windsor, Inc. Recalls Meat and Poultry Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V285000·2016-05-11

    Forest River Recalls 2016-2017 Berkshire and Cross Country RVs for Sway Bar Defect

    Forest River is recalling specific 2016-2017 Berkshire and 2016 Cross Country recreational vehicles because front sway bar brackets may not fit properly, risking detachment and crashes.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN BERKSHIRE, CROSS COUNTRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1606-2016·2016-05-11

    CareFusion Alaris PC Unit Model 8015 Recalled for Power-Up Error

    CareFusion 303, Inc. is recalling 23,397 Alaris PC units, Model 8015, because a super capacitor failure may cause a system error code at power-up.

    Product
    Alaris PC unit, Model 8015 The Alaris PC unit is the central programming, monitoring and power supply component for the Alaris System.
    Category
    Medical Device
    Distribution
    Distributed nationwide